| Literature DB >> 28805964 |
Sarah Allegra1, Giovanna Fatiguso1, Silvia De Francia2, Fabio Favata1, Elisa Pirro2, Chiara Carcieri1, Amedeo De Nicolò1, Jessica Cusato1, Giovanni Di Perri1, Antonio D'Avolio1.
Abstract
Voriconazole therapeutic drug monitoring is not consistently recommended due to its high interpatient and intrapatient variability. Here, we aimed to describe our experience with voriconazole for treatment and prophylaxis of invasive fungal infections in paediatric patients. A fully validated high-performance liquid chromatography-mass spectrometry method was used to quantify voriconazole concentration in plasma, at the end of dosing interval. A high interindividual variability was shown. We enrolled 237 children, 83 receiving intravenous and 154 oral voriconazole. A positive correlation between drug dose and drug plasma exposure was observed. Considering intravenous route, patients with higher serum creatinine had higher voriconazole concentrations; a positive correlation was found among drug exposure and age. Sex significantly influenced drug levels: males had higher median drug concentrations than females (P < 0.001). Close voriconazole pharmacokinetics monitoring should help individualize antifungal therapy for children.Entities:
Keywords: antifungals; high-performance liquid chromatography; invasive fungal infections; therapeutic drug monitoring; triazoles
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Year: 2017 PMID: 28805964 PMCID: PMC5736853 DOI: 10.1111/bcp.13401
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335